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Ex vivo susceptibility-weighted imaging anatomy of canine brain–comparison of imaging and histological sections
Now that access of large domestic mammals to high-field MRI becomes more common, techniques initially implemented for human patients can be used for the structural and functional study of the brain of these animals. Among them, susceptibility-weighted imaging (SWI) is a recent technique obtained fro...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9481421/ https://www.ncbi.nlm.nih.gov/pubmed/36124091 http://dx.doi.org/10.3389/fnana.2022.948159 |
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author | Arribarat, Germain Cartiaux, Benjamin Boucher, Samuel Montel, Charles Gros-Dagnac, Hélène Fave, Yoann Péran, Patrice Mogicato, Giovanni Deviers, Alexandra |
author_facet | Arribarat, Germain Cartiaux, Benjamin Boucher, Samuel Montel, Charles Gros-Dagnac, Hélène Fave, Yoann Péran, Patrice Mogicato, Giovanni Deviers, Alexandra |
author_sort | Arribarat, Germain |
collection | PubMed |
description | Now that access of large domestic mammals to high-field MRI becomes more common, techniques initially implemented for human patients can be used for the structural and functional study of the brain of these animals. Among them, susceptibility-weighted imaging (SWI) is a recent technique obtained from gradient echo (GE) imaging that allow for an excellent anatomical tissue contrast and a non-invasive assessment of brain iron content. The goal of this study was to design an optimal GE SWI imaging protocol to be used in dogs undergoing an MRI examination of the brain in a 3-Tesla scanner. This imaging protocol was applied to ex vivo brains from four dogs. The imaging protocol was validated by visual inspection of the SWI images that provided a high anatomical detail, as demonstrated by their comparison with corresponding microscopic sections. As resolvable brain structures were labeled, this study is the first to provide an anatomic description of SWI images of the canine brain. Once validated in living animals, this GE SWI imaging protocol could be easily included in routine neuroimaging protocols to improve the diagnosis of various intracranial diseases of dogs, or be used in future comparative studies aiming at evaluating brain iron content in animals. |
format | Online Article Text |
id | pubmed-9481421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94814212022-09-18 Ex vivo susceptibility-weighted imaging anatomy of canine brain–comparison of imaging and histological sections Arribarat, Germain Cartiaux, Benjamin Boucher, Samuel Montel, Charles Gros-Dagnac, Hélène Fave, Yoann Péran, Patrice Mogicato, Giovanni Deviers, Alexandra Front Neuroanat Neuroscience Now that access of large domestic mammals to high-field MRI becomes more common, techniques initially implemented for human patients can be used for the structural and functional study of the brain of these animals. Among them, susceptibility-weighted imaging (SWI) is a recent technique obtained from gradient echo (GE) imaging that allow for an excellent anatomical tissue contrast and a non-invasive assessment of brain iron content. The goal of this study was to design an optimal GE SWI imaging protocol to be used in dogs undergoing an MRI examination of the brain in a 3-Tesla scanner. This imaging protocol was applied to ex vivo brains from four dogs. The imaging protocol was validated by visual inspection of the SWI images that provided a high anatomical detail, as demonstrated by their comparison with corresponding microscopic sections. As resolvable brain structures were labeled, this study is the first to provide an anatomic description of SWI images of the canine brain. Once validated in living animals, this GE SWI imaging protocol could be easily included in routine neuroimaging protocols to improve the diagnosis of various intracranial diseases of dogs, or be used in future comparative studies aiming at evaluating brain iron content in animals. Frontiers Media S.A. 2022-09-02 /pmc/articles/PMC9481421/ /pubmed/36124091 http://dx.doi.org/10.3389/fnana.2022.948159 Text en Copyright © 2022 Arribarat, Cartiaux, Boucher, Montel, Gros-Dagnac, Fave, Péran, Mogicato and Deviers. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Arribarat, Germain Cartiaux, Benjamin Boucher, Samuel Montel, Charles Gros-Dagnac, Hélène Fave, Yoann Péran, Patrice Mogicato, Giovanni Deviers, Alexandra Ex vivo susceptibility-weighted imaging anatomy of canine brain–comparison of imaging and histological sections |
title | Ex vivo susceptibility-weighted imaging anatomy of canine brain–comparison of imaging and histological sections |
title_full | Ex vivo susceptibility-weighted imaging anatomy of canine brain–comparison of imaging and histological sections |
title_fullStr | Ex vivo susceptibility-weighted imaging anatomy of canine brain–comparison of imaging and histological sections |
title_full_unstemmed | Ex vivo susceptibility-weighted imaging anatomy of canine brain–comparison of imaging and histological sections |
title_short | Ex vivo susceptibility-weighted imaging anatomy of canine brain–comparison of imaging and histological sections |
title_sort | ex vivo susceptibility-weighted imaging anatomy of canine brain–comparison of imaging and histological sections |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9481421/ https://www.ncbi.nlm.nih.gov/pubmed/36124091 http://dx.doi.org/10.3389/fnana.2022.948159 |
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